The following data is part of a premarket notification filed by Smith & Nephew, Inc. with the FDA for Smith & Nephew Modular Hip.
Device ID | K052426 |
510k Number | K052426 |
Device Name: | SMITH & NEPHEW MODULAR HIP |
Classification | Prosthesis, Hip, Semi-constrained, Uncemented, Metal / Polymer, Non-porous, Calcium Phosphate |
Applicant | SMITH & NEPHEW, INC. 1450 E BROOKS ROAD Memphis, TN 38116 |
Contact | Jason Sells |
Correspondent | Jason Sells SMITH & NEPHEW, INC. 1450 E BROOKS ROAD Memphis, TN 38116 |
Product Code | MEH |
CFR Regulation Number | 888.3353 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-09-02 |
Decision Date | 2005-12-07 |
Summary: | summary |